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WormBase Tree Display for Variation: WBVar01465284

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Name Class

WBVar01465284EvidencePaper_evidenceWBPaper00040707
NamePublic_nameWBVar01465284
Other_nameCE41189:p.Ala69=
ZK228.4a.1:c.162T>C
ZK228.4c.1:c.90T>C
ZK228.4b.1:c.207T>C
CE16713:p.Ala54=
CE47905:p.Ala30=
HGVSgCHROMOSOME_V:g.18463521T>C
Sequence_detailsSMapS_parentSequenceZK228
Flanking_sequencesAGCAGGAGTTTCCCTGGCCCGCTGGGACGCAAAAATGACGGACCCCTCTACTCAATTGGC
Mapping_targetZK228
Type_of_mutationSubstitutiontc
SeqStatusSequenced
Variation_typeSNP
Natural_variant
OriginSpeciesCaenorhabditis elegans
StrainWBStrain00005299From_analysisWGS_Andersen
WBStrain00005300From_analysisWGS_Andersen
WBStrain00005307From_analysisWGS_Andersen
LaboratoryQX
PersonWBPerson1730
AnalysisWGS_Andersen
DB_infoDatabasedbSNP_rsrs193350940
dbSNP_ssss295526859
StatusLive
AffectsGeneWBGene00013947
TranscriptZK228.4b.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK228.4b.1:c.207T>C
HGVSpCE41189:p.Ala69=
cDNA_position235
CDS_position207
Protein_position69
Exon_number3/8
Codon_changegcT/gcC
Amino_acid_changeA
ZK228.4c.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK228.4c.1:c.90T>C
HGVSpCE47905:p.Ala30=
cDNA_position206
CDS_position90
Protein_position30
Exon_number3/8
Codon_changegcT/gcC
Amino_acid_changeA
ZK228.4a.1VEP_consequencesynonymous_variant
VEP_impactLOW
HGVScZK228.4a.1:c.162T>C
HGVSpCE16713:p.Ala54=
cDNA_position183
CDS_position162
Protein_position54
Exon_number3/8
Codon_changegcT/gcC
Amino_acid_changeA
ReferenceWBPaper00040707
MethodWGS_Andersen